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view sam_dump.xml @ 22:751a694ec620 draft
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit 1db2b3ee758847b8b63f58fb2075961003ff8c22"
author | iuc |
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date | Mon, 20 Jul 2020 07:27:41 -0400 |
parents | 494b2ec08162 |
children | 653e89d73fc4 |
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<tool id="sam_dump" name="Download and Extract Reads in BAM" version="@VERSION@+galaxy2" profile="18.01"> <description>format from NCBI SRA</description> <macros> <import>sra_macros.xml</import> </macros> <expand macro="requirements"> <requirement type="package" version="1.10">samtools</requirement> </expand> <version_command>sam-dump --version</version_command> <command detect_errors="exit_code"> <![CDATA[ @COPY_CONFIGFILE@ @SET_ACCESSIONS@ ## Do not use prefetch if region is specified, to avoid downloading ## the complete sra file. #if $input.input_select == "file": sam-dump --log-level fatal '${input.file.name}' #else: #if ( str( $adv.region ) == "" ): prefetch -X 200000000 "\$acc" && #end if sam-dump --log-level fatal --disable-multithreading #end if #if str( $adv.region ) != "": --aligned-region '$adv.region' #end if #if str( $adv.matepairDist ) != "": --matepair-distance '$adv.matepairDist' #end if #if str( $adv.minMapq ) != "": --min-mapq '$adv.minMapq' #end if --header #if str( $adv.alignments ) == "both": --unaligned #end if #if str( $adv.alignments ) == "unaligned": --unaligned-spots-only #end if #if (str( $adv.primary ) == "yes") and (str ( $adv.alignments != "unaligned") ): --primary #end if #if $input.input_select == "file": '$input.file' #elif $input.input_select == "accession_number": "\$acc" #elif $input.input_select=="file_list": "\$acc" #end if #if str( $outputformat ) == "bam": | samtools view -Sb - 2> /dev/null #end if #if $input.input_select == "file": > '$output_file' #elif $input.input_select == "accession_number": > '$output_accession' ) #end if #if $input.input_select=="file_list": #if str( $outputformat ) == "bam": > "\$acc.bam" #elif str( $outputformat ) == "sam": > "\$acc.sam" #end if ) ; done #end if ]]> </command> <expand macro="configfile_hack"/> <inputs> <expand macro="input_conditional"/> <param name="outputformat" type="select" display="radio" label="select output format" help="In vast majority of cases you want to download data in bam format. It is more compact and is accepted by all downstream tools."> <option value="bam">bam</option> <option value="sam">sam</option> </param> <section name="adv" title="Advanced Options" expanded="False"> <expand macro="alignments"/> <expand macro="region"/> <expand macro="matepairDist"/> <param name="primary" type="select" value="no"> <label>only primary aligments</label> <option value="no">No</option> <option value="yes">Yes</option> </param> <expand macro="minMapq"></expand> </section> </inputs> <outputs> <collection name="output_collection" type="list" label="SAM/BAM data (fastq-dump)"> <filter>input['input_select'] == "file_list"</filter> <discover_datasets pattern="(?P<designation>.+)\.bam" directory="." ext='bam'/> <discover_datasets pattern="(?P<designation>.+)\.sam" directory="." ext='sam'/> </collection> <data name="output_accession" format="bam" label="${input.accession} (sam-dump)"> <filter>input['input_select'] == "accession_number"</filter> <change_format> <when input="outputformat" value="sam" format="sam"/> </change_format> </data> <data name="output_file" format="bam" label="${input.file.name} (sam-dump)"> <filter>input['input_select'] == "file"</filter> <change_format> <when input="outputformat" value="sam" format="sam"/> </change_format> </data> </outputs> <tests> <test> <param name="input_select" value="accession_number"/> <param name="accession" value="SRR925743"/> <param name="outputformat" value="sam"/> <param name="region" value="17:41243452-41277500"/> <output name="output_accession" file="sam_dump_result.sam" compare="contains" ftype="sam"/> </test> </tests> <help><![CDATA[ **What it does?** This tool extracts data (in BAM_ format) from the Short Read Archive (SRA) at the National Center for Biotechnology Information (NCBI). It is based on the sam-dump_ utility of the SRA Toolkit. **How to use it?** There are three ways in which you can download data: 1. Data for single accession 2. Multiple datasets using a list of accessions 3. Extract data from already uploaded SRA dataset Below we discuss each in detail. ------ **Uploading data for a single accession** When you type a single accession number (e.g., `SRR1582967`) into **Accession** box and click **Execute** the tool will fetch data for you. As a result you will get a single BAM (or SAM) dataset in the history. ----- **Uploading multiple datasets using a list of accessions** A more realistic scenario is when you want to upload a number of datasets at once. To do this you need a list of accession, where there is only one accession per line (see below for information on how to generate such a file). Once you have this file: 1. Upload it into your history using Galaxy's upload tool 2. Once the list of accessions is uploaded choose *List of SRA accessions, one per line* from **select input type** dropdown 3. Choose uploaded file within the **sra accession list** field 4. Click **Execute** .. class:: warningmark BAM datasets produced by this option will be saved in Galaxy's history as a collection_ - a single history element containing multiple datasets. ----- **Extract data from already uploaded SRA dataset** If a SRA dataset is present in the history, it can be converted into BAM dataset by setting **select input type** drop-down to *SRA archive in current history*. Just like in the case of extracting data for single accession number a single BAM dataset will be generated in the history. @ACCESSION_LIST_HOWTO@ ----- .. _BAM: https://samtools.github.io/hts-specs/SAMv1.pdf .. _sam-dump: https://ncbi.github.io/sra-tools/sam-dump.html .. _collection: https://galaxyproject.org/tutorials/collections/ .. _link: https://trace.ncbi.nlm.nih.gov/Traces/sra/sra.cgi?view=studies @SRATOOLS_ATTRRIBUTION@ ]]></help> <expand macro="citation"/> </tool>